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Bioscience, Biotechnology, and Biochemistry Volume 71, 2007 - Issue 11
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Original Articles

Parvitexins A–E, Clerodane-Type Diterpenes Isolated from the in Vitro-Cultured Liverwort, Scapania parvitexta

Kinya KATAYAMADepartment of Veterinary Science, Nippon Veterinary and Life Science University
,
Kazuko SHIMAZAKIDepartment of Veterinary Science, Nippon Veterinary and Life Science University
,
Hiroyuki TAZAKIDepartment of Veterinary Science, Nippon Veterinary and Life Science University
,
Yasuhiro HASADepartment of Bioresource Science, Obihiro University of Agriculture and Veterinary Medicine
,
Masako MIYOSHIDepartment of Bioresource Science, Obihiro University of Agriculture and Veterinary Medicine
,
Hiroyuki KOSHINOThe Institute of Physical and Chemical Research (RIKEN)
,
Tatsuo FURUKINatural History Museum & Institute
&
Kensuke NABETADivision of Applied Life Science, Graduate School of Agriculture, Hokkaido University
 show all
Pages 2751-2758 | Received 06 Jun 2007, Accepted 12 Jul 2007, Published online: 22 May 2014

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  • 2) Nagashima, F., and Asakawa, Y., Rearranged cuparane-type sesqui- and Clerodane-type diterpenoids from the liverwort Demotarisia linguifolia. Phytochemistry, 29, 3229–3231 (1990).
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  • 7) Tazaki, H., Becker, H., and Nabeta, K., Seco-clerodane diterpenoids jamesoniellides H, I and J in axenic cultures of the liverwort Jamesoniella autumnalis. Phytochemistry, 51, 743–750 (1999).
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  • 12) Takeda, R., and Katoh, K., Growth and sesquiterpenoid production by Calypogeia granulata Inoue cells in suspension culture. Planta, 151, 525–530 (1981).
  • 13) Goto, H., and Osawa, E., An efficient algorithm for searching low-energy conformers of cyclic and acyclic molecules. J. Chem. Soc., Perkin Trans. 2, 187–198 (1993).
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  • 16) Lii, J. H., and Allinger, N. L., Molecular mechanics. The MM3 force field for hydrocarbons. 3. The van der Waals’ potentials and crystal data for aliphatic and aromatic hydrocarbons. J. Am. Chem. Soc., 111, 8576–8582 (1989).
  • 17) Ohtani, I., Kusumi, T., Kashman, Y., and Kakisawa, H., High-field FT NMR application of Mosher’s method. The absolute configuration of marine terpenoids. J. Am. Chem. Soc., 113, 4092–4096 (1991).
  • 18) Asakawa, Y., “Progress in the Chemistry of Organic Natural Products” Vol. 65, eds. Herz, W., Kirby, G. W., Moore, R. E., Steglich, W., and Tamm, C., Springer, Vienna, pp. 1–618 (1995).
  • 19) de la Torre, M. C., Bruno, M., Piozzi, F., Savon, G., Omar, A. A., Perales, A., and Rodríguez, B., Two neo-clerodane diterpenoids containing an unusual 2,6-dioxabicyclo[2.2.1]heptane structural moiety. Tetrahedron, 47, 3463–3470 (1991).

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